Author: Victoria White, Digital Content Producer
May 23, 2016
Safinamide is available for the treatment of adult patients with
idiopathic Parkinson’s disease (PD) as an add-on therapy to a stable dose of
Levodopa (L-dopa) alone or in combination with other Parkinson’s disease
medicines in mid-to late-stage fluctuating patients.
Safinamide is a new chemical entity with a unique mode of action
including selective and reversible MAO-B-inhibition and blocking of voltage
dependent sodium channels which leads to modulation of abnormal glutamate
release. Clinical trials have established its efficacy in controlling motor
symptoms and motor complications in the short term, with data supporting this
effect over 2 years. Results from 6 month double-blind controlled studies
suggest that safinamide shows statistically significant effects on motor
fluctuations (ON/OFF time) without increasing the risk of developing
troublesome dyskinesia. Safinamide is a once-daily dose and has no diet
restrictions.
Safinamide now available in eight countries
Commenting on the availability of the treatment, Andrew Lees, MD
FRCP, FMedSci, Professor of Neurology, (The National Hospital for Neurology and
Neurosurgery, Queen Square and Emeritus Director, Reta Lila Weston Institute of
Neurological Studies, University College London, Institute of Neurology), said:
“After 10 years with no new drugs for Parkinson’s disease I welcome the
addition of another effective treatment option for patients.”
Maurizio Castorina, CEO of Zambon, added: “We are committed to
developing innovative therapies for patients suffering from PD and other
central nervous system diseases. Xadago offers PD patients a novel therapeutic
option in the treatment of this progressive disease.”
The UK is the latest country launching safinamide, which is also
available in seven other countries: Germany, Switzerland, Spain, Italy,
Belgium, Denmark, and Sweden.
http://www.europeanpharmaceuticalreview.com/41218/news/industry-news/parkinsons-disease-safinamide/?
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